Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Curable thiol-ene compositions for optical articles

a technology of thiol-ene compositions and optical articles, applied in the field of curable thiolene compositions, can solve the problems of optical defects, unpredictability of registration, net shrinkage in volume, etc., and achieve the effects of low birefringence, low shrinkage, and rapid photocuration

Inactive Publication Date: 2009-04-21
3M INNOVATIVE PROPERTIES CO
View PDF33 Cites 24 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0006]The present invention includes a photopolymerizable composition comprising an aliphatic urethane (meth)acrylate oligomer, a polythiol, optionally a reactive diluent, and optionally a photoinitiator. The inventive composition can be made free of solvent and unreactive species and can be rapidly photocured. The composition, when cured is non-yellowing, exhibits low shrinkage and low birefringence making it suitable for many optical applications such as optical lenses, optical fibers, prisms, light guides, optical adhesives, and optical films.
[0008]Advantageously, the present invention provides curable compositions that are readily melt processible without appreciable monomers, reactive diluents and photoinitiators. Curable systems containing a significant amount of solvent, monomers and reactive diluents can give rise to a significant increase in density when transformed from the uncured to the cured state causing a net shrinkage in volume. As is well known, shrinkage can cause unpredictable registration in precise molding operations such as those required in manufacture of optical elements such as lenses. Shrinkage can also create residual stress in such optical articles, which can subsequently lead to optical defects, including high birefringence.

Problems solved by technology

Curable systems containing a significant amount of solvent, monomers and reactive diluents can give rise to a significant increase in density when transformed from the uncured to the cured state causing a net shrinkage in volume.
As is well known, shrinkage can cause unpredictable registration in precise molding operations such as those required in manufacture of optical elements such as lenses.
Shrinkage can also create residual stress in such optical articles, which can subsequently lead to optical defects, including high birefringence.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Curable thiol-ene compositions for optical articles
  • Curable thiol-ene compositions for optical articles

Examples

Experimental program
Comparison scheme
Effect test

examples

[0064]These examples are for illustrative purposes only and are not meant to be limiting on the scope of the appended claims. All parts, percentages, ratios, etc. in the examples and the rest of the specification are by weight, unless noted otherwise. Solvents and other reagents used were obtained from Sigma-Aldrich Chemical Company; Milwaukee, Wis. unless otherwise noted.

[0065]

Table of AbbreviationsAbbreviation ofTrade NameDescriptionPETMPPentaerythritol tetrakis(3-mercaptopropionate) availablefrom Dow Chemical Company, Midland, MITMPTMPTrimethylolpropane tris(3-mercaptopropionate)available from Dow Chemical Company, Midland, MICN1963Aliphatic urethane methacrylate oligomer containing25% TMPTMA as reactive diluent available fromSartomer Company Inc, Exton, PAPro7327Aliphatic urethane methacrylate oligomer containing noreactive diluent (i.e. CN1963 without TMPTMA)available from Sartomer Company Inc, Exton, PATMPTMATrimethylolpropane trimethacrylate, SR350, availablefrom Sartomer Com...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Tgaaaaaaaaaa
thicknessaaaaaaaaaa
shrinkageaaaaaaaaaa
Login to View More

Abstract

Curable thiol-ene compositions containing urethane (meth)acrylate oligomers that are readily polymerized to produce optical articles and coatings are described.

Description

FIELD OF THE INVENTION[0001]The present invention provides curable thiol-ene compositions containing urethane (meth)acrylate oligomers that are readily polymerized to produce optical articles and coatings.BACKGROUND OF THE INVENTION[0002]Radiation curable compositions containing carbon-carbon unsaturated monomers and polythiols were developed in the early 1970s. U.S. Pat. No. 4,234,676 (Hein et al.) describe a composition comprising a carbon-carbon unsaturated polymer, a crosslinkable monomer, a polythiol, and curing agent directed primarily at printing plate production.[0003]U.S. Pat. No. 4,808,638 (Steinkraus, et al) describes a composition comprising a norbornene resin, polythiol, and free radical initiator that can be photocured in visible light when an iron arene complex is present.[0004]U.S. Pat. No. 4,139,385 (Crivello) describes a composition comprising a polyolefin, polythiol, and onium salt photoinitiator. The films, 75 micrometers thick (3 mil), were curable by a cationic...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(United States)
IPC IPC(8): B29C35/08C08J3/28G02B1/04C08G18/67C08G75/04
CPCC08F2/46C08G18/672C08G75/045C09D175/16C08G18/83C08G18/42C08G18/87C08G75/04
Inventor CHENG, MINGOLOFSON, PETER M.CRATON, MICHELE A.LU, YING-YUH
Owner 3M INNOVATIVE PROPERTIES CO
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products